1,004 Qa Manager jobs in the United Kingdom

An established Steel & Architectural Metalwork company in Kent is seeking an experienced Health and Safety / QA Manager to join their team immediately.

Important details:

• Salary: £50,000 - £65,000
• Package: Company car, mobile phone, company pension scheme, 28 days paid annual leave + Bank Holidays
• Working hours are from Monday - Friday, 8AM til 5PM

Key Responsibilities

• All aspects of H & S for workshop and site operations
• Implementing new procedures and processes and managing the OHSM system
• Accident and incident reporting RIDDOR
• Site safety inspections
• Attend customer H & S meetings and conferences
• Managing staff training programme
• Fire safety and Risk management
• Producing and managing RAMS
• QA Procedures in terms of UKCA Accreditation
• QA Procedures in terms of Factory Production Control
• QA recording and sign-off

Key Qualifications

• NEBOSH Certificate (General or Construction) - Required
• Proven H&S and QA management experience in steel/construction
• Strong knowledge of UK H&S regulations (CDM 2015, RIDDOR)
• Experience with OHSMS (ISO 45001), UKCA Accreditation, and FPC
• Ability to produce and manage RAMS, site safety inspections, and audits
• Strong communication skills for training and H&S meetings

Please apply with your most up to date CV and you will be contacted

QA/RA Manager – Medical Devices

We are seeking an enthusiastic QA/RA Manager with a strong background in medical devices and regulatory compliance to support a London-based client . You will lead the development and operation of the Quality Management System (QMS), support IT/data security, and implement regulatory strategies to maintain compliance and enable product commercialization.

Key Responsibilities:

• Implement and maintain the QMS, including Document Control, Non-Conformance, CAPA, and audit programs
• Ensure alignment with medical device standards and regulations: ISO 13485:2016, ISO 14971:2019, IEC 62304, IEC 60601, UK MDR 2002, EU MDR 2017/745, FDA QSR
• Manage supplier and service provider compliance
• Oversee Design Control, Risk Management, and quality metrics reporting
• Support regulatory submissions (UKCA/CE, FDA, clinical/research studies)
• Promote a strong quality culture and coordinate IT, information security, and Health & Safety activities

Requirements:

• Degree in Life Sciences, Engineering, or related field (or equivalent industrial experience)
• Proven experience managing QMS and compliance in medical devices (hardware & software)
• Strong knowledge and application of medical device standards and global regulatory frameworks
• Experience with electronic QMS software and internal auditing
• Experience contributing to regulatory submissions and interacting with notified/regulatory bodies
• Previous experience in oncology preferred
• Strong leadership, collaboration, and stakeholder management skills

Desirable:

• Data protection or information security experience
• Health & Safety training (e.g., IOSH Managing Safely)

Benefits:

• Share options
• Private medical and dental cover
• 5% employer pension contribution
• Life and health insurance
• Lunch provided at work
• Flexible working (minimum 2 days/week in office)
• 25 days annual leave
• Bonus scheme linked to company milestones
• Opportunities for learning and professional development

If this position could be of interest apply, or reach out on:

+44 (0)

QA/RA Manager – Medical Devices

We are seeking an enthusiastic QA/RA Manager with a strong background in medical devices and regulatory compliance to support a London-based client . You will lead the development and operation of the Quality Management System (QMS), support IT/data security, and implement regulatory strategies to maintain compliance and enable product commercialization.

Key Responsibilities:

• Implement and maintain the QMS, including Document Control, Non-Conformance, CAPA, and audit programs
• Ensure alignment with medical device standards and regulations: ISO 13485:2016, ISO 14971:2019, IEC 62304, IEC 60601, UK MDR 2002, EU MDR 2017/745, FDA QSR
• Manage supplier and service provider compliance
• Oversee Design Control, Risk Management, and quality metrics reporting
• Support regulatory submissions (UKCA/CE, FDA, clinical/research studies)
• Promote a strong quality culture and coordinate IT, information security, and Health & Safety activities

Requirements:

• Degree in Life Sciences, Engineering, or related field (or equivalent industrial experience)
• Proven experience managing QMS and compliance in medical devices (hardware & software)
• Strong knowledge and application of medical device standards and global regulatory frameworks
• Experience with electronic QMS software and internal auditing
• Experience contributing to regulatory submissions and interacting with notified/regulatory bodies
• Previous experience in oncology preferred
• Strong leadership, collaboration, and stakeholder management skills

Desirable:

• Data protection or information security experience
• Health & Safety training (e.g., IOSH Managing Safely)

Benefits:

• Share options
• Private medical and dental cover
• 5% employer pension contribution
• Life and health insurance
• Lunch provided at work
• Flexible working (minimum 2 days/week in office)
• 25 days annual leave
• Bonus scheme linked to company milestones
• Opportunities for learning and professional development

If this position could be of interest apply, or reach out on:

+44 (0)

QA Compliance Manager - South East England
About the Company Join a global diagnostics manufacturer renowned for its innovation, quality, and impact in the life sciences sector. With a network of modern manufacturing facilities and a growing international footprint, the company is investing heavily in transformation and continuous improvement. You'll be part of a collaborative culture that offers clear career progression, training opportunities, and a shared commitment to improving patient outcomes.
About the Role We're hiring a QA Compliance Manager to lead a team focused on maintaining and enhancing the Quality Management System (QMS) in compliance with GMP, ISO 9001, ISO 13485, and other regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits, while also supporting regulatory inspections, training, and change control.This is a senior-level opportunity with potential Qualified Person (QP) sponsorship for the right candidate.
Key Responsibilities:

• Lead and develop the QA Compliance team
• Maintain and improve the QMS in line with EU GMP and ISO standards
• Oversee internal audits, CAPA management, and batch documentation review
• Host customer audits and support regulatory inspections
• Drive continuous improvement and contribute to strategic quality initiatives
• Support training, change control, and compliance projects

Candidate Requirements Essential:

• Degree in a scientific discipline (e.g. Chemistry, Biology, or related field)
• 10+ years' experience in GMP-regulated environments
• Strong leadership and people management skills
• In-depth knowledge of EU cGMP, ISO 9001, and ISO 13485
• Experience supporting or conducting batch release under QP supervision
• Lead Auditor training and a proactive approach to quality improvement
• Excellent communication, organisation, and stakeholder engagement skills

Desirable:

• Experience in diagnostics or medical device manufacturing
• Familiarity with regulatory inspections (e.g. MHRA, FDA, ISO audits)

What's on Offer

• Competitive salary and benefits
• Clear progression pathway with potential QP sponsorship
• Opportunity to shape quality strategy in a transforming global business

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

Job Summary:

Intertek is supporting a major infrastructural project in Riyadh, contributing to broader national development initiatives that promote sustainable growth and public interest in line with Saudi Arabia’s Vision 2030.

As part of this program, Intertek will deliver advisory and analytical services to strengthen regulations, codes, guidelines, policies, procedures, governance, and stakeholder alignment across permitting, licensing, inspections, and municipal services.

Key Responsibilities:

• Lead and manage technical reviews, validations, and approvals across relevant disciplines, ensuring compliance with applicable codes, standards, and masterplans.
• Collaborate with internal teams, consultants, and stakeholders to ensure efficient execution of permitting, licensing, inspection, and design compliance processes.
• Implement and maintain robust quality assurance and control systems, conduct audits, and ensure all deliverables meet regulatory and performance standards.
• Identify gaps and inefficiencies in workflows, develop and implement process improvements, and standardize operating procedures to enhance overall effectiveness.
• Interpret technical codes and regulations, provide guidance on waivers, and support resolution of complex engineering and design challenges.
• Prepare and present regular progress reports, maintain transparent documentation, and monitor operational activities using digital performance dashboards.
• Establish clear communication protocols with staff, applicants, and external partners, and ensure stakeholder feedback is captured and addressed.
• Support training, mentorship, and knowledge transfer initiatives to build team capacity and contribute to succession planning.
• Ensure availability of necessary resources, tools, and systems to support successful project delivery, and promote automation and digital integration where applicable.

Requirements

Qualifications:

• BSc or MSc degree in relevant engineering or technical discipline.
• Candidates should have significant professional experience working in Western Europe or with major corporations headquartered in that region.
• Minimum 10-15 years of experience in the subject field with a strong record of achievements.
• Proven ability to lead full programs and multidisciplinary teams.
• Strong universal engineering background across technical domains.
• Excellent proficiency in discipline-specific software tools.

Benefits:

• Long-term contract of 5+ years, with the possibility of renewal.
• Fully remote position, offering flexibility and global collaboration.
• Includes ad hoc business trips to Saudi Arabia as required.
• The selected candidate will be hired under an Intertek contract, ensuring professional engagement and support.

Requisition ID:  60790
Position Type:  FT Fixed Term
Workplace Arrangement:  #LI-Onsite

About Kerry

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.

Our Safety purpose: At Kerry, we work together in a caring culture where everybody goes home safe every day. We are committed to providing a safe working environment and ensuring that all safety protocols are strictly followed. Join us in creating a workplace where safety is everyone's responsibility.

About the role

This is a fixed-term, onsite position based in Portadown, Northern Ireland , running until the end of August 2026 , with the potential for extension.

The site specialises in the production of cheese blocks, sliced cheese, and grated cheese bags.

As a Quality Control Technician , you will support the technical team by conducting routine inspections, monitoring production processes, and ensuring compliance with food safety standards. You’ll assist with audits, equipment calibrations, data reporting, and documentation management. The role also involves cross-functional collaboration to uphold site standards and contribute to quality improvement initiatives. 

Key responsibilities

As a Quality Control Technician, you will:

• Play a key role in maintaining product integrity and food safety standards

• Conduct routine inspections and monitor production processes

• Support the technical team with problem-solving on the factory floor

• Assist with equipment calibrations and preparation for external audits

• Carry out internal audits including glass & perspex, pest control, and temperature checks

• Trend and report data, including results from the daily Taste Panel

• Manage samples, traceability documentation, and ensure technical records are audit-ready

• Collaborate with all departments to uphold site standards

• Contribute to ongoing quality improvement initiatives across the site

• Perform other day-to-day tasks as requested to support quality and technical operations

Qualifications and skills

• Experience in a food manufacturing or quality control environment

• Solid understanding of food safety standards and regulatory compliance

• Familiarity with laboratory testing methods and equipment

• Competence in using Microsoft Office and quality management systems (e.g., SAP, QMS)

What we offer

• 25 days annual leave (excluding bank holidays)

• Matched pension scheme

• Access to our employee development platform and Udemy learning resources

• Benefits platform offering discounts and cashback at major retailers

• A collaborative and inclusive work environment with opportunities for career growth

Kerry is an Equal Opportunities Employer.  Consistent with our policy of providing equality of opportunity for all, we are required to seek particular information from applicants.  As part of your application you will be asked to answer a short number of questions.  This information will be held separate to your application and treated in the strictest of confidence. 

Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. 

Recruiter:  #LI-MU1 
Posting Type:  LI 

We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.

In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.

Benefits:

• This is a full-time or part-time REMOTE position
• You’ll be able to choose which projects you want to work on
• You can work on your own schedule
• Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work

Responsibilities:

• Give AI chatbots diverse and complex chemistry problems and evaluate their outputs
• Evaluate the quality produced by AI models for correctness and performance

Qualifications:

• A current, in progress, or completed Masters and/or PhD is preferred but not required
• Fluency in English (native or bilingual level)
• Detail-oriented
• Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning

Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.